Caffeine Citrate Injection, Solution
Product Images NDC 63323-407

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Caffeine Citrate (NDC 63323-407). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Structural Formula (Caf02 0003 01)

Structural Formula (Caf02 0003 01)
Chemical structure of caffeine citrate depicting the molecular formula C14H18N4O9 and molecular weight 386.31. The diagram shows the caffeine molecule alongside the citrate molecule, accurately representing their combined chemical structure.*
FDA Label Image

Logo (Caf02 0003 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY)

Package Label (PRINCIPAL DISPLAY)
Label for Caffeine Citrate Injection USP, 60 mg per 3 mL (20 mg per mL) in a 3 mL single-dose vial for intravenous use only. The label states it is sterile, nonpyrogenic, preservative-free, and for single use. Manufactured by Fresenius Kabi USA, LLC in Lake Zurich, IL, with storage instructions and a barcode.*
FDA Label Image

Ppackage Label (PRINCIPAL DISPLAY)

Ppackage Label (PRINCIPAL DISPLAY)
Label for Caffeine Citrate Injection, USP 20 mg/mL (60 mg per 3 mL) intravenous solution by Fresenius Kabi USA, LLC. The single-dose vial label includes dosage strength, preservative-free status, storage instructions, and barcode. The label states it is sterile, nonpyrogenic, for single use only, and contains a detailed ingredient list and usage conditions.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.